N-terminal, internal, and C-terminal peptide modifications are useful for a variety of applications, such as Western blotting, protein-protein interaction studies, and fluorescence-based assays. Use the table below for a list of various applications and to jump to more information, including structures and relevant references.
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Carbamidomethylation (CAM) is a deliberate post-translational modification introduced to cysteine residues by reacting with iodoacetamide. Peptides with this modification are mainly used in Peptide Mass Fingerprinting for identification and characterization of proteins1. In other assays, this process is used to block Cysteine from oxidation2.
AQUA peptides are synthetic peptides with amino acids enriched in 18O, 13C, and/or 14N. They are similar to their native peptides in terms of chemical, physical properties and also their biological activities1. Main applications for these peptides are to study protein interactions, proteins, post translation modifications such as ubiquitination and phosphorylation2-5.
Phosphorylation can be performed on Tyr, Ser and Thr residues as a posttranslational modification (PTM) on peptides. Phosphorylated peptides have application in many cellular processes such as gene expression, protein-protein interaction and signal transduction in plants and animals1,2.
Spacers are used to create a distance between the peptide and the cargo to reduce steric hindrance at the binding sites of the peptide. In this case cargo can be a drug, dye, tag.
Attachment of poly (ethylene glycol) to a peptide is called PEGylation. Short bifunctional PEG (Poly (ethylene glycol)) can be used as a spacer in bioconjugation of peptides with other molecules. PEG bioconjugation has also been used to improve proteolytic stability, biodistribution and solubility of peptides1-2.
The C-terminal of the peptide is synthesized as an amide to neutralize negative charge created by the C-terminal COOH. This modification is added to prevent enzyme degradation, to mimic native proteins, and in some cases to remove hydrogen bonding at the C-terminal of the peptides which may interfere with the assays.1
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